Citation

Mai Pham LT, Kim SJ, Kim YH. Biotechnology for Biofuels 2016; 9(1).

Copyright

(Copyright © 2016)

DOI

10.1186/s13068-016-0664-1

PMID

unavailable

Abstract

BACKGROUND: Although lignin peroxidase is claimed as a key enzyme in enzyme-catalyzed lignin degradation, in vitro enzymatic degradation of lignin was not easily observed in lab-scale experiments. It implies that other factors may hinder the enzymatic degradation of lignin. Irreversible interaction between phenolic compound and lignin peroxidase was hypothesized when active enzyme could not be recovered after the reaction with degradation product (guaiacol) of lignin phenolic dimer.

RESULTS: In the study of lignin peroxidase isozyme H8 from white-rot fungi Phanerochaete chrysosporium (LiPH8), W251 site was revealed to make the covalent coupling with one moiety of monolignolic radical (guaiacol radical) by LC-MS/MS analysis. Hypothetical electron-relay containing W251 residue was newly suggested based on the observation of repressed radical coupling and remarkably lower electron transfer rate for W215A mutant. Furthermore, the retardation of the suicidal radical coupling between the W251 residue and the monolignolic radical was attempted by supplementing the acidic microenvironment around the W251 residue to engineer radical-robust LiPH8. Among many mutants, mutant A242D showed exceptional catalytic performances by yielding 21.1- and 4.9-fold higher increases of kcat and kcat/KM values, respectively, in the oxidation of non-phenolic model lignin dimer.

CONCLUSIONS: A mechanism-based suicide inhibition of LiPH8 by phenolic compounds was firstly revealed and investigated in this work. Radical-robust LiPH8 was also successfully engineered by manipulating the transient radical state of radical-susceptible electron-relay. Radical-robust LiPH8 will play an essential role in degradation of lignin, which will be consequently linked with improved production of sugars from lignocellulose biomass. © The Author(s) 2016.

Language: un

Keywords

Isoenzymes; mass spectrometry; Degradation; Suicide inhibition; Phenols; Free radical reactions; catalysis; Lithium compounds; Lithium Compounds; Electron transitions; Alcohols; Fungi; degradation; enzyme; Lignin; cellulose; Cellulose; biomass; Acidic microenvironment; Catalytic oxidation; Catalytic performance; Electron transfer rates; Enzymatic Degradation; fungus; inductively coupled plasma method; lignin; Lignin peroxidase; Lignin peroxidase isozyme H8; Long-range electron transfer; Phanerochaete chrysosporium; Radical coupling